Gabapentin

Product NDC

55154-7149

11-digit product format

551547149

Labeler code

55154

Product ID

55154-7149_d55972f3-8990-404b-a837-e592cf4955b0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Gabapentin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Cardinal Health

Application

ANDA078926

Marketing category

ANDA

Marketing start

2014-09-01

Marketing end

2020-08-31

Substance

GABAPENTIN

Active strength

800 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record